Medical Device Manufacturer · CH , Baar

Schiller AG - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1985

Recent clearances: ARGUS PB-3000, CARDIOVIT AT-102 G2

16

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Schiller AG Cardiovascular ✕

14 devices

1-14 of 14

Cleared Jul 06, 2023

Cardiovascular · 451d

Cleared Mar 02, 2020

CARDIOVIT AT-102 G2

Cardiovascular · 447d

Cleared Jul 19, 2017

Cardiovascular · 177d

Cleared May 06, 2016

Diagnostic Station DS20

Cardiovascular · 288d

Cleared Nov 12, 2010

WELCH ALLYN 1500 PATIENT MONITOR

Cardiovascular · 156d

Cleared Mar 07, 2007

Cardiovascular · 75d

Cleared May 19, 2006

ARGUS, MODEL LCM

Cardiovascular · 184d

Cleared Aug 09, 2005

BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM

Cardiovascular · 76d

Cleared May 04, 2005

CARDIOVIT AT-10PLUS

Cardiovascular · 49d

Cleared Aug 24, 2004

MONITORING SYSTEM, MODEL ARGUS PB-2200

Cardiovascular · 270d

Cleared Apr 14, 2004

CARDIOVIT AT-102

Cardiovascular · 331d

Cleared Apr 08, 2002

MONITORING SYSTEM,MODEL ARGUS PB-1000

Cardiovascular · 266d

Cleared Apr 25, 1985

CARDIOVIT CS-6 ECG-RECORDER

Cardiovascular · 63d

Cleared Jan 24, 1985

Cardiovascular · 304d